Annals of Pediatric Endocrinology & Metabolism

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"Most Download" Articles are updated quarterly. Below are Ann Pediatr Endocrinol Metab’s most frequently downloaded articles for the previous last months.


The association between idiopathic scoliosis and growth hormone treatment in short children (96 times): Mijin Park, Yu Jin Kim, Kyeong Eun Oh, Eungu Kang, Hyo-Kyoung Nam, Young-Jun Rhie, Kee-Hyoung Lee; Ann Pediatr Endocrinol Metab. 2022;27(3):207-213. Published online May 16, 2022; DOI: https://doi.org/10.6065/apem.2142186.093
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report (49 times): Sung Eun Kim, Na Yeong Lee, Won Kyoung Cho, Jisook Yim, Jae Wook Lee, Myungshin Kim, Jae Hee Chung, Min Ho Jung, Byung-Kyu Suh, Moon Bae Ahn; Ann Pediatr Endocrinol Metab. 2022;27(4):315-319. Published online January 17, 2022; DOI: https://doi.org/10.6065/apem.2142100.050; Full text PubReader ePub Crossref - TDM PDF


Endocrinal dysfunction in children with Down syndrome (135 times): Kotb Abbass Metwalley, Hekma Saad Farghaly; Ann Pediatr Endocrinol Metab. 2022;27(1):15-21. Published online March 31, 2022; DOI: https://doi.org/10.6065/apem.2142236.118
Cited By 2; Full text PubReader ePub Crossref - TDM PDF


Growth plate extracellular matrix defects and short stature in children (29 times): Maria Alessandra Saltarelli, Alessia Quarta, Francesco Chiarelli; Ann Pediatr Endocrinol Metab. 2022;27(4):247-255. Published online December 31, 2022; DOI: https://doi.org/10.6065/apem.2244120.060; Full text PubReader ePub Crossref - TDM PDF


Two cases of 17α-hydroxylase/17,20-lyase deficiency caused by the CYP17A1 mutation (153 times): Hae In Lee, Ahreum Kwon, Jung Hwan Suh, Han Saem Choi, Kyung Chul Song, Hyun Wook Chae, Ho-Seong Kim; Ann Pediatr Endocrinol Metab. 2021;26(1):66-70. Published online March 31, 2021; DOI: https://doi.org/10.6065/apem.2040184.092
Cited By 3; Full text PubReader ePub Crossref - TDM PDF


Low serum 25-hydroxyvitamin D level is associated with obesity and atherogenesis in adolescent boys (103 times): Junko Naganuma, Satomi Koyama, Osamu Arisaka, Shigemi Yoshihara; Ann Pediatr Endocrinol Metab. 2022;27(1):30-36. Published online October 17, 2021; DOI: https://doi.org/10.6065/apem.2142112.056
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


Balanced assessment of growth disorders using clinical, endocrinological, and genetic approaches (127 times): Martin Oswald Savage, Helen Louise Storr; Ann Pediatr Endocrinol Metab. 2021;26(4):218-226. Published online December 31, 2021; DOI: https://doi.org/10.6065/apem.2142208.104
Cited By 6; Full text PubReader ePub Crossref - TDM PDF


Clinical management and emerging therapies of FGFR3-related skeletal dysplasia in childhood (92 times): Hwa Young Kim, Jung Min Ko; Ann Pediatr Endocrinol Metab. 2022;27(2):90-97. Published online June 30, 2022; DOI: https://doi.org/10.6065/apem.2244114.057
Cited By 1; Full text PubReader ePub Crossref - TDM PDF


The association between C-reactive protein, metabolic syndrome, and prediabetes in Korean children and adolescents (44 times): Ji Hyun Kim, Jung Sub Lim; Ann Pediatr Endocrinol Metab. 2022;27(4):273-280. Published online June 28, 2022; DOI: https://doi.org/10.6065/apem.2142226.113; Full text PubReader ePub Crossref - TDM PDF


Commentary on “Growth plate extracellular matrix defects and short stature in children” (24 times): Se Young Kim; Ann Pediatr Endocrinol Metab. 2022;27(4):243-244. Published online December 31, 2022; DOI: https://doi.org/10.6065/apem.2222060edi03; Full text PubReader ePub Crossref - TDM PDF

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